A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209675



Internal ID22357714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81433852..81433981hg38UCSC Ensembl
chr6:82143569..82143698hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14328750
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209675
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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